- Mohr–
Tranebjærg syndrome (MTS) is a rare X-linked
recessive syndrome also
known as deafness–dystonia
syndrome and
caused by
mutation in the TIMM8A gene...
-
Tranebjaerg–Svejgaard syndrome, also
known as X-linked
mental ****ation ****ociated with
psoriasis is a very rare
genetic disorder which is characterized...
- membrane. The gene is
mutated in deafness-dystonia
syndrome (or Mohr-
Tranebjaerg syndrome; MTS/DFN-1) and it is
postulated that MTS/DFN-1 is a mitochondrial...
-
disease Genetic disorders: Qazi–Markouizos syndrome, Say–Meyer syndrome,
Tranebjaerg-Svejgaard syndrome, Wiedemann–Steiner syndrome, Wilson's disease, etc...
-
Mesial temporal sclerosis,
pattern of
hippocampal neuron cell loss Mohr–
Tranebjærg syndrome, also
known as deafness–dystonia
syndrome MTS ****ay, a biochemical...
- HC; Cambon-Thomsen, A; Knoppers, BM; Meijers-Heijboer, H; Scheffer, H;
Tranebjaerg, L; Dondorp, W; de Wert, GM (June 2013). "Whole-genome
sequencing in...
-
Korkko J,
Czarny M,
Warman ML,
Brunner HG,
Kaariainen H,
Mulliken JB,
Tranebjaerg L,
Brooks DG, Cox GF,
Cruysberg JR,
Curtis MA,
Davenport SL, Friedrich...
- Hsieh, M.; Nicholson, G. A.; Brunt, E.; Higgins, J. J.; Lauritzen, M.;
Tranebjaerg, L.; Volpini, V.; Wood, N.; Ranum, L.; Tsuji, S.; Brice, A.; Sequeiros...
-
Tracheoesophageal fistula Tracheophageal fistula hypospadias Trachoma Tranebjaerg–Svejgaard
syndrome Transcobalamin II
deficiency Transient erythroblastopenia...
- 1-2-3-lqt.unipv.it.
Retrieved 2024-01-17. "Genotype risk relationship".
Tranebjaerg L,
Bathen J,
Tyson J, Bitner-Glindzicz M (September 1999). "Jervell and...
